Measuring and Interpreting Nuclear Transport in Neurodegenerative Disease—The Example of C9orf72 ALS

Transport from and into the nucleus is essential to all eukaryotic life and occurs through the nuclear pore complex (NPC). There are a multitude of data supporting a role for nuclear transport in neurodegenerative diseases, but actual transport assays in disease models have provided diverse outcomes. In this review, we summarize how nuclear transport works, which transport assays are available, and what matters complicate the interpretation of their results. Taking a specific type of ALS caused by mutations in C9orf72 as an example, we illustrate these complications, and discuss how the current data do not firmly answer whether the kinetics of nucleocytoplasmic transport are altered. Answering this open question has far-reaching implications, because a positive answer would imply that widespread mislocalization of proteins occurs, far beyond the reported mislocalization of transport reporters, and specific proteins such as FUS, or TDP43, and thus presents a challenge for future research.


Nucleocytoplasmic Transport
Nucleocytoplasmic transport (NCT) occurs through nuclear pore complexes (NPCs), large protein complexes embedded in the nuclear membrane. NPCs facilitate and regulate the import and export of proteins and RNA between the nucleus and cytoplasm. Small proteins will rapidly diffuse through the NPC, but the passage of larger molecules is hindered by the NPC's permeability barrier [1,2]. The association of proteins or RNAs with specific importins, exportins, and transportins, grouped together as nuclear transport receptors (NTRs), facilitates the passage of macromolecules, large and small, across the barrier (Figure 1).
The NPC is made up of proteins called nucleoporins (Nups) that build the cylindrical structure embedded in the nuclear membrane. FG-Nups containing phenylalanine-glycine (FG) repeats constitute roughly half of the mass of the NPCs [3] with about 200 copies of FG-Nups found in each pore [3,4]. The precise nature of the permeability barrier formed by the FG-Nups is still under debate, but what is clear is that the NTRs associate directly with the FG-Nups, even with specificity to certain Nups over others [5][6][7][8][9][10], to facilitate the passage of NTR-cargo complexes. Additionally, a pool of importin-β functions as a stable component of the NPC's permeability barrier [11]. The differential localization of NPC-associated proteins in a single yeast nucleus suggests that NPCs may even have specialized transport functions [12].
In baker's yeast, there are 19 known NTR [13][14][15][16], whereas in human cells, 30 NTRs [17] are identified. The substrate specificity of some, but not all NTRs has been mapped, and jointly they bind a large and diverse group of cargoes, while some redundancies exist [18]. The importin-β superfamily is the largest class of NTRs; they can either directly bind to Figure 1. Nucleocytoplasmic transport can be measured with fluorophore-tagged transport reporters. (A) GFP tagged with an NLS accumulates in the nucleus owing to constant active import, which is faster than the passive leak in the opposite direction. (B) GFP tagged with an NES accumulates in the cytosol owing to constant active export, which overpowers passive influx. (C) GFP tagged with both an NLS and NES sequence accumulates depending on the strongest signal, as it is both actively imported and exported and passively diffuses across the nuclear pore. Passive diffusion (=influx and efflux) is dependent on the concentration gradient of the reporter, the number of NPCs, and their permeability. (A) GFP tagged with an NLS accumulates in the nucleus owing to constant active import, which is faster than the passive leak in the opposite direction. (B) GFP tagged with an NES accumulates in the cytosol owing to constant active export, which overpowers passive influx. (C) GFP tagged with both an NLS and NES sequence accumulates depending on the strongest signal, as it is both actively imported and exported and passively diffuses across the nuclear pore. Passive diffusion (=influx and efflux) is dependent on the concentration gradient of the reporter, the number of NPCs, and their permeability.
Ran, a member of the Ras family of small GTPases, is in its GTP bound state in the nucleus and its GDP bound state in the cytosol. This gradient functions to ensure that the cargoes are accumulated in the nucleus or cytosol by promoting the removal of cargo from importins and the loading of cargo to exportins [22][23][24]. Whereas importins bind to either the NLS of their cargo or to the RanGTP, exportins bind to both the NES of their cargo and the RanGTP cooperatively. Therefore, cargo release from importins depends on RanGTP binding, while cargo release from exportins needs RanGTP hydrolysis. RanGTP levels in the nucleus are maintained by the guanine nucleotide exchange factor RCC1 or RanGEF. RanGTP is converted to RanGDP in the cytoplasm by the GTPase-activating protein RanGAP. NCT is thus an interplay between the NPCs, with a number of different NTRs recognizing cargo through sorting signals and a gradient of Ran in its GTP or GDP bound state.

Amyotrophic Lateral Sclerosis (ALS)
ALS is a neurodegenerative disease that affects neurons in the brain and spinal cord. Amyotrophy is the degeneration of spinal motor neurons, which leads to denervation and muscle wasting. Lateral sclerosis refers to the scarring (sclerosis) of the lateral axons, which control voluntary movement [25]. In most cases, the cause for ALS remains unknown, but Nuclear accumulation (N/C) is decreased (dose-dependent and more so with PR 20 /GR 20 than with PR 10 /GR 10 ), and minimal decrease with GA 10 /PA 10 Nuclear accumulation (N/C) is unchanged (GP 10 ) Hayes 2020 [50] IBB-domain KPNA2 -FRET sensor (nuclear) Impβ DPR Peptide injection in permeabilized HeLa cells Nuclear accumulation (N/C) is decreased (more so with PR 20 /GR 20 than with PR 10 /GR 10 ) † † † Nuclear accumulation (N/C) is unchanged (PA 10 /GA 10 /GP 10 ) GST-GFP-NLS Sv40 (nuclear) Impα/β complex Nuclear accumulation (N/C) is decreased (more so with PR 20 /GR 20 than with PR 10 /GR 10 ) Nuclear accumulation (N/C) is unchanged (PA 10 /GA 10 /GP 10 ) Nuclear accumulation (N/C) is decreased (more so with PR 20 /GR 20 than with PR 10 /GR 10 ) Nuclear accumulation (N/C) is unchanged (PA 10 /GA 10 /GP 10 ) Impα/β complex DPR peptide addition to medium HeLa cells Nuclear accumulation (N/C) is decreased (GR 25 ) ‡ ‡ * K to P mutation in the PKI-NES. † PR 175 -GFP was lower expressed than the GFP-GR 149 and GA 149 -GFP. † † Reduced protein translation for GR 100 /PR 100 expressing cells. † † † Passive diffusion of GFP and small fluorescent dextrans into the nuclei of permeabilized HeLa cells increased by PR 10 and GR 10 , not by GP 10 , GA 10 , or PA 10 . ‡ Nuclear with dexamethasone. ‡ ‡ Nuclear accumulation and solubility of control GCR 2 -GFP 2 reporter (lacking NLS) not altered.

Commonly Used Nuclear Transport Assays
The assays monitoring the kinetics of nuclear import and/or export generally use small inert reporters, such as GFP with a sorting signal, to control and limit reporter retention [60]. A GFP-NES or GFP-NLS reporter will passively pass the NPC down the concentration gradient owing to its small size, but additionally be actively transported owing to the NES/NLS [60]. Thus, its localization at steady state is the result of continuous nuclear import and efflux in the case of GFP-NLS, and export and influx in the case of GFP-NES (see Figure 1). The ratio between the fluorescence levels in the nucleus and cytosol provides the most common transport readout (the N/C ratio). The steady state localization of reporters encoding both an NLS and NES report on the ratio between import and export [61]. Provided that proper controls for the functionality of the NLS and NES are performed, this strategy has the advantage that, with a single cell line/model, one can monitor both import and export.
To measure actual rates of transport and influx/efflux, there are several strategies. Influx rates can be measured by monitoring the passive nuclear entry of larger cargoes, e.g., multimers of GFP, of proteinA, and of maltose-binding protein moieties [1,2]. The passive diffusion through the pores is affected by the overall size and shape of the protein, and its surface properties [62]. For example, surface histidines, cysteines, and arginines will facilitate the movement through the FG-Nup meshwork, and higher surface hydrophobicity increases the NPC passage [62]. Efflux and influx rates can also be measured using the GFP-NLS and GFP-NES reporters by inhibiting active import or export and following the subsequent loss of compartmentalisation. Import and export rates are derived from experiments where the import or export of GFP-NLS or GFP-NES reporters is temporarily disturbed, after which the re-establishment of the equilibrium can be quantified. Jointly, this collection of assays reports on the steady state ratios between nuclear entry and exit, or yields the individual rates of entry and exit by temporarily altering the steady state.
There are several options to block import or export. CRM1 export can be inhibited by Leptomicin B (LMB) [63], a fungicide that binds CRM1 irreversibly in the NES binding region, thus blocking the binding between CRM1 and its cargo [64,65]. A limitation of the use of LMB may be its off-target effects; it also inhibits the degradation of p53 and upregulates apoptosis in cancer lines [66], limits RNA translation [67], and leads to accumulation of poly(A) + RNA within the nucleus [68]. Several import inhibitors are available that each block a specific transport route; e.g., importazole [69], ivermectin [70], and free importin-β-binding domain [50] inhibit the importin-α/β route, while the M9M peptide inhibits TNPO1 [71]. Alternatively, 2-deoxyglucose and/or sodium azide deplete cells from ATP, and can thus also be used to disrupt the RanGTP gradient. Depleting RanGTP inhibits major export and import pathways, but the different export routes are more sensitive to RanGTP depletion than the import via importin-α, importin-β, or transportin [72]. Especially in baker's yeast, inhibition of import has been accomplished by anchor away strategies, such as anchoring of Kap95 to the plasma membrane ATPase using rapamycin inducible dimerization of FRB-and FKBP-domains attached to the NTR and the plasma membrane ATPase [73]. Methods that are performed at steady state and circumvent the use of drugs or poisons are based on fluorescence recovery after photobleaching (FRAP) and fluorescence loss in photobleaching (FLIP). In import studies, the nuclear area is bleached, and the recovery of nuclear fluorescence, which relies on the exchange of fluorescent molecules from the cytosol with bleached molecules from the nuclear compartments, is taken as a read-out for import rates [74,75]. As all assays, except those based on FRAP and FLIP, are subject to possible side effects of the interventions inhibiting transport, a combination of interventions is advisable.
Commonly used nucleocytoplasmic transport assays are performed in permeabilized cells, in live cells, or in in vitro assembled oocyte nuclei, and are listed in Table 2. A much used in vitro NCT assay uses digitonin permeabilized cells supplemented with exogenous recombinant transport factors [76]. This assay yields nuclei with functional NPCs while allowing to introduce the reporter proteins and NTRs at known concentrations and timepoints. The disadvantages are that permeabilization can relocate or extract soluble proteins [77] including transport factors and ATP [76], and potentially alter transport kinetics. In order to limit method artefacts, permeabilization assays are preferably combined with live-cell imaging [77]. The simplest transport measurements in live cells are those that determine the steady state distribution of GFP-NLS or GFP-NES reporters. Alternatively, as discussed above, the kinetics can be determined either based on the use of poisons to alter the steady state, or based on FRAP or FLIM. Lastly, like permeabilized cells, in vitro assembled oocyte nuclei also provide a system where reporter proteins and NTRs can be introduced at known concentrations and timepoints aiding kinetic measurements. Xenopus egg extracts contain the structural components of nuclei in a disassembled state, but will reconstitute nucleus-like structures around added DNA [78]. These nuclei actively exclude nonnuclear proteins and accumulate nucleoplasmin and proteins with NLSs [79][80][81], and import can be inhibited with lectin wheat germ agglutin, which binds to glycosylated FG-Nups [82]. Here, a combination of transport models may also provide the best assessment of the question at hand. that determine the steady state distribution of GFP-NLS or GFP-NES reporters. Alternatively, as discussed above, the kinetics can be determined either based on the use of poisons to alter the steady state, or based on FRAP or FLIM. Lastly, like permeabilized cells, in vitro assembled oocyte nuclei also provide a system where reporter proteins and NTRs can be introduced at known concentrations and timepoints aiding kinetic measurements. Xenopus egg extracts contain the structural components of nuclei in a disassembled state, but will reconstitute nucleus-like structures around added DNA [78]. These nuclei actively exclude nonnuclear proteins and accumulate nucleoplasmin and proteins with NLSs [79][80][81], and import can be inhibited with lectin wheat germ agglutin, which binds to glycosylated FG-Nups [82]. Here, a combination of transport models may also provide the best assessment of the question at hand. Cell permeabilization + Allows addition of specific concentration of cargo/NTR [76,83] -Permeabilization can relocate or extract soluble proteins [77] including transport factors/ATP [76]; might deplete NTRs from NPCs; and reduces concentrations of competitive cargo, which increases import rates [84] In vivo N/C ratios; use of inhibitors + N/C ratio is a robust read-out largely independent of reporter levels [85] -Expression/injection of reporter might be toxic; use of inhibitors to measure rates of nuclear entry and exit might be toxic In vivo FRAP/FLIP + Direct measurement of kinetics of nuclear entry and exit; area under the curve indicates mobile fraction of the reporter -Expression/injection of reporter might be toxic; photobleaching induces ROS Xenopus egg extracts + Proteins can be added to/immunodepleted from the extract -No native cytosolic fraction ·Allows studying nuclear pore complex assembly, function [86], transport [87,88], and cargo competition [89].

Nuclear Transport Up-Close: Complications when Interpreting Nuclear Transport Data
NCT assays rely on monitoring the localization of proteins to either the nuclear or cytosolic compartment ( Figure 1). A change in localization can report a change in import or export efficiency by the joint action of NPCs, NTRs, and Ran. The interpretation of what drives the change in import or export efficiency and the contribution of each specific component (NPCs, NTRs or Ran), however, is often complicated for a number of reasons.
First, cargoes are transported by dedicated transporters, which recognize their cargo via particular NLSs and/or NESs. However, often, a simple "one cargo-one NTR" relation does not exist, as specific NTR-isoforms show preference for certain NLSs, several NTRs can be redundant for one specific NLS, and a protein or protein complex can contain multiple localization sequences (see Table 3 for examples). NLS sequences are, among others, the classical NLS, which has a mono-or bipartite basic amino acid cluster [90]; the PY-Cell permeabilization + Allows addition of specific concentration of cargo/NTR [76,83] -Permeabilization can relocate or extract soluble proteins [77] including transport factors/ATP [76]; might deplete NTRs from NPCs; and reduces concentrations of competitive cargo, which increases import rates [84] Int. J. Mol. Sci. 2021, 22, x FOR PEER REVIEW 7 of 24 that determine the steady state distribution of GFP-NLS or GFP-NES reporters. Alternatively, as discussed above, the kinetics can be determined either based on the use of poisons to alter the steady state, or based on FRAP or FLIM. Lastly, like permeabilized cells, in vitro assembled oocyte nuclei also provide a system where reporter proteins and NTRs can be introduced at known concentrations and timepoints aiding kinetic measurements. Xenopus egg extracts contain the structural components of nuclei in a disassembled state, but will reconstitute nucleus-like structures around added DNA [78]. These nuclei actively exclude nonnuclear proteins and accumulate nucleoplasmin and proteins with NLSs [79][80][81], and import can be inhibited with lectin wheat germ agglutin, which binds to glycosylated FG-Nups [82]. Here, a combination of transport models may also provide the best assessment of the question at hand. Cell permeabilization + Allows addition of specific concentration of cargo/NTR [76,83] -Permeabilization can relocate or extract soluble proteins [77] including transport factors/ATP [76]; might deplete NTRs from NPCs; and reduces concentrations of competitive cargo, which increases import rates [84] In vivo N/C ratios; use of inhibitors + N/C ratio is a robust read-out largely independent of reporter levels [85] -Expression/injection of reporter might be toxic; use of inhibitors to measure rates of nuclear entry and exit might be toxic In vivo FRAP/FLIP + Direct measurement of kinetics of nuclear entry and exit; area under the curve indicates mobile fraction of the reporter -Expression/injection of reporter might be toxic; photobleaching induces ROS Xenopus egg extracts + Proteins can be added to/immunodepleted from the extract -No native cytosolic fraction ·Allows studying nuclear pore complex assembly, function [86], transport [87,88], and cargo competition [89].

Nuclear Transport Up-Close: Complications when Interpreting Nuclear Transport Data
NCT assays rely on monitoring the localization of proteins to either the nuclear or cytosolic compartment (Figure 1). A change in localization can report a change in import or export efficiency by the joint action of NPCs, NTRs, and Ran. The interpretation of what drives the change in import or export efficiency and the contribution of each specific component (NPCs, NTRs or Ran), however, is often complicated for a number of reasons.
First, cargoes are transported by dedicated transporters, which recognize their cargo via particular NLSs and/or NESs. However, often, a simple "one cargo-one NTR" relation does not exist, as specific NTR-isoforms show preference for certain NLSs, several NTRs can be redundant for one specific NLS, and a protein or protein complex can contain multiple localization sequences (see Table 3 for examples). NLS sequences are, among others, the classical NLS, which has a mono-or bipartite basic amino acid cluster [90]; the PY-In vivo N/C ratios; use of inhibitors + N/C ratio is a robust read-out largely independent of reporter levels [85] -Expression/injection of reporter might be toxic; use of inhibitors to measure rates of nuclear entry and exit might be toxic that determine the steady state distribution of GFP-NLS or GFP-NES reporters. Alternatively, as discussed above, the kinetics can be determined either based on the use of poisons to alter the steady state, or based on FRAP or FLIM. Lastly, like permeabilized cells, in vitro assembled oocyte nuclei also provide a system where reporter proteins and NTRs can be introduced at known concentrations and timepoints aiding kinetic measurements. Xenopus egg extracts contain the structural components of nuclei in a disassembled state, but will reconstitute nucleus-like structures around added DNA [78]. These nuclei actively exclude nonnuclear proteins and accumulate nucleoplasmin and proteins with NLSs [79][80][81], and import can be inhibited with lectin wheat germ agglutin, which binds to glycosylated FG-Nups [82]. Here, a combination of transport models may also provide the best assessment of the question at hand.  [77] including transport factors/ATP [76]; might deplete NTRs from NPCs; and reduces concentrations of competitive cargo, which increases import rates [84] In vivo N/C ratios; use of inhibitors + N/C ratio is a robust read-out largely independent of reporter levels [85] -Expression/injection of reporter might be toxic; use of inhibitors to measure rates of nuclear entry and exit might be toxic In vivo FRAP/FLIP + Direct measurement of kinetics of nuclear entry and exit; area under the curve indicates mobile fraction of the reporter -Expression/injection of reporter might be toxic; photobleaching induces ROS Xenopus egg extracts + Proteins can be added to/immunodepleted from the extract -No native cytosolic fraction ·Allows studying nuclear pore complex assembly, function [86], transport [87,88], and cargo competition [89].

Nuclear Transport Up-Close: Complications when Interpreting Nuclear Transport Data
NCT assays rely on monitoring the localization of proteins to either the nuclear or cytosolic compartment (Figure 1). A change in localization can report a change in import or export efficiency by the joint action of NPCs, NTRs, and Ran. The interpretation of what drives the change in import or export efficiency and the contribution of each specific component (NPCs, NTRs or Ran), however, is often complicated for a number of reasons.
First, cargoes are transported by dedicated transporters, which recognize their cargo via particular NLSs and/or NESs. However, often, a simple "one cargo-one NTR" relation does not exist, as specific NTR-isoforms show preference for certain NLSs, several NTRs can be redundant for one specific NLS, and a protein or protein complex can contain multiple localization sequences (see Table 3 for examples). NLS sequences are, among others, the classical NLS, which has a mono-or bipartite basic amino acid cluster [90]; the PY- that determine the steady state distribution of GFP-NLS or GFP-NES reporters. Alternatively, as discussed above, the kinetics can be determined either based on the use of poisons to alter the steady state, or based on FRAP or FLIM. Lastly, like permeabilized cells, in vitro assembled oocyte nuclei also provide a system where reporter proteins and NTRs can be introduced at known concentrations and timepoints aiding kinetic measurements. Xenopus egg extracts contain the structural components of nuclei in a disassembled state, but will reconstitute nucleus-like structures around added DNA [78]. These nuclei actively exclude nonnuclear proteins and accumulate nucleoplasmin and proteins with NLSs [79][80][81], and import can be inhibited with lectin wheat germ agglutin, which binds to glycosylated FG-Nups [82]. Here, a combination of transport models may also provide the best assessment of the question at hand.  [77] including transport factors/ATP [76]; might deplete NTRs from NPCs; and reduces concentrations of competitive cargo, which increases import rates [84] In vivo N/C ratios; use of inhibitors + N/C ratio is a robust read-out largely independent of reporter levels [85] -Expression/injection of reporter might be toxic; use of inhibitors to measure rates of nuclear entry and exit might be toxic In vivo FRAP/FLIP + Direct measurement of kinetics of nuclear entry and exit; area under the curve indicates mobile fraction of the reporter -Expression/injection of reporter might be toxic; photobleaching induces ROS Xenopus egg extracts + Proteins can be added to/immunodepleted from the extract -No native cytosolic fraction ·Allows studying nuclear pore complex assembly, function [86], transport [87,88], and cargo competition [89].

Nuclear Transport Up-Close: Complications when Interpreting Nuclear Transport Data
NCT assays rely on monitoring the localization of proteins to either the nuclear or cytosolic compartment (Figure 1). A change in localization can report a change in import or export efficiency by the joint action of NPCs, NTRs, and Ran. The interpretation of what drives the change in import or export efficiency and the contribution of each specific component (NPCs, NTRs or Ran), however, is often complicated for a number of reasons.
First, cargoes are transported by dedicated transporters, which recognize their cargo via particular NLSs and/or NESs. However, often, a simple "one cargo-one NTR" relation does not exist, as specific NTR-isoforms show preference for certain NLSs, several NTRs can be redundant for one specific NLS, and a protein or protein complex can contain multiple localization sequences (see Table 3 for examples). NLS sequences are, among others, the classical NLS, which has a mono-or bipartite basic amino acid cluster [90]; the PY-Xenopus egg extracts + Proteins can be added to/immunodepleted from the extract -No native cytosolic fraction ·Allows studying nuclear pore complex assembly, function [86], transport [87,88], and cargo competition [89].

Nuclear Transport Up-Close: Complications When Interpreting Nuclear Transport Data
NCT assays rely on monitoring the localization of proteins to either the nuclear or cytosolic compartment (Figure 1). A change in localization can report a change in import or export efficiency by the joint action of NPCs, NTRs, and Ran. The interpretation of what drives the change in import or export efficiency and the contribution of each specific component (NPCs, NTRs or Ran), however, is often complicated for a number of reasons.
First, cargoes are transported by dedicated transporters, which recognize their cargo via particular NLSs and/or NESs. However, often, a simple "one cargo-one NTR" relation does not exist, as specific NTR-isoforms show preference for certain NLSs, several NTRs can be redundant for one specific NLS, and a protein or protein complex can contain multiple localization sequences (see Table 3 for examples). NLS sequences are, among others, the classical NLS, which has a mono-or bipartite basic amino acid cluster [90]; the 7 of 21 PY-NLS; and a RG-rich NLS [91]. Some importins have their own preferred sequences, such as yeast Kap121, which recognizes a non-conventional lycine-rich sequence [92]. There is not yet a full overview in which sequences are recognized by the importins, but attempts are ongoing to discover more NLSs [93]. The full complement of interactions between NTRs and cargoes in a specific cellular setting has not been established to date, hence a change in localization of one cargo cannot easily be connected to the activity of a specific NTR or NTR isoform.
Second, import rates depend on the availability of the NTRs [84,94,95]. The formation of a complex of NTR and cargo in the crowded cytosol is rate-limiting compared with the fast translocation through the NPC, which is reported to occur on the timescale of milliseconds for commonly used reporters [96]. Therefore, altering the concentration of NTRs impacts transport rates. For example, Kap121 and Kap123 recognize the same NLSs, and when expressed at similar concentrations, import rates are indistinguishable [84]. However, natively, the abundance of Kap123 is higher than that of Kap121, thus making Kap123mediated import faster [84]. Import rates eventually saturate at high NTR levels, which must be owing to saturation of the NPCs, the RanGTP transport complex dissociation, or both [84]. The expression or availability of NTRs can change under stress conditions. For example, the importin Hikeshi, which uses ATP to import Hsp70 to limit shock-induced damage, is specifically upregulated under heat stress [16]. Moreover, conditions of oxidative stress and heat shock lead to rapid accumulation of Impα in the nucleus [97,98], and arsenite stress accumulates Impα in stress granules [99]. To explain a change in the localization of a reporter mechanistically, one would want to know whether the intervention, e.g., the introduction of DPRs or G 4 C 2 DNA sequences, created a change in the levels of NTRs available for transport. Table 3. Transport specificity and redundancy. Lycine-rich sequence [92] Attempts to discover more NLSs [93] CRM1

I. Transport of Cargo Depends on a Localization Sequence that is Recognized by an NTR
where Φ is I, M, F, V, and mostly L [105,106] PKI: e.g., MSLNELALKLAGLDI [58] HIV-1 Rev: LQLPPLERLTL

III. Redundancy in NTRs for One Type of Cargo NTR1
NLSi -Cargo1 NTR2 NLSii-Cargo1 A group of cargoes, with distinct NLSs, can be recognized by different NTRs; e.g., Kap121 can substitute Kap123 for import of ribosomal proteins [111,112]
One cargo may contain an NLS and an NES; cyclin B [118,119] and HIV Rev [105,120] contain an impβ1 NLS and a CRM1 NES.
Third, import rates also depend on the affinity between NTR and NLS, where over a certain range, a higher affinity will give a higher import rate [84,85,123]. However, a too high binding affinity prevents NTR-cargo complex dissociation and, consequently, inhibits transport [124,125]. Affinities can be temporarily altered by post-translational modifications (PTM), with phosphorylation of NTRs [126,127] and NLSs [128,129], the most studied PTM regulating NCT [130,131]. For example, transcription factors are only required for short periods of time and in small amounts, and sequences close to their NLS are phosphorylated to increase the affinity for importins [128,129] or cause retention in nucleus or cytoplasm [132]. However, methylation [133,134], ubiquitination [135][136][137], acetylation [138], and sumoylation [139] have also been shown to influence NTR binding. NTR binding can also be altered by physicochemical parameters, as is the case for ROSinduced formation of disulfide bonds between TRN1 and FOXO [140], which is reversed in the more reduced environment of the nucleus [141]. Proteolytic events can unmask NLS and NES sequences [142][143][144], whereas binding to another protein [145][146][147] or mRNA [148], or protein multimerization [149,150], can bury sorting sequences. To explain a change in the localization of a reporter mechanistically, one would want to know whether the affinity of the NTR for the NLS is altered. This is often not trivial to determine as the affinities determined with purified protein can be different from those determined in cytoplasmic extract [151] or those observed when multiple cargoes are presented simultaneously [152].
A fourth, and major, complication to interpret what drives the change in import or export efficiency is related to the fact that nuclear import of a specific heterologously expressed transport reporter (Figure 1) is always in competition with the transport of native cargoes. Because most NTRs have more than one specific cargo to transport, an increase in any of the cargoes of that NTR leads to lower N/C ratios of all its cargoes, including the reporter used to study transport [75,89]. Additionally, more cargo for one NTR can limit RanGTP availability to all NTRs, and slow down the recycling of importins and export. These aspects are easily overlooked when interpreting NCT data, but can lead to the false conclusion that the import kinetics by one specific NTR is reduced in a disease model compared with a wild type situation, while all that is changing is the concentration of competing cargo.
Lastly, it should be taken into account that changes in the localization of a reporter can be the result of changes to the NPCs themselves, both in number and in functionality. Recently, a disease-related reduced nuclear abundance of key Nups was shown in C9ALS and sporadic ALS iPSNs [153]. Theoretical considerations predict that fewer NPCs will support a higher accumulation of a GFP-NLS reporter in the nucleus [154], as the number of NPCs is likely limiting for efflux, but not for import [84,89]. Additionally, the deletion of one nucleoporin immediately translates to reduced export [155][156][157][158][159][160][161], but because the rate limiting step for import is receptor binding [95,154,162], cells still maintain high import rates even when FG-domains in the NPCs are deleted [6,163]. Specific NTRs preferentially bind specific FG-Nups, hence the presence or absence of certain FG-Nups may affect only specific import routes [6,164,165]. PTM has been reported to change the structure of pores. For example, in yeast, phosphorylation of Nup53 releases its binding partner Nup170, thus exposing binding sites for Kap121 on Nup170, limiting Kap121 import directly [166], a process that may also underlie reduced transport by TRN-1 and Kapβ [127]. Knowing the number and functionality of individual NPCs is a major challenge, and together with the previously mentioned complications of mapping the full complement of NTRS and cognate cargoes in a cell, these aspects provide the largest challenge in interpreting what underlies a change in the localization of a NCT reporter.
To summarize, in order to assess if the transport of proteins is altered in a disease model, well controlled steady state, or dynamic measurements of the location of mobile, non-toxic reporter proteins suffice. Preferably, multiple NLS-or NES-containing reporters representing different transport pathways are used. To understand what drives a possible change in the transport of these reporters, several additional, and rather complex, questions have to be addressed (summarized in Figure 2). In case of the outermost layers, we enter into what is presently still largely uncharted scientific territory. rate limiting step for import is receptor binding [95,154,162], cells still maintain high import rates even when FG-domains in the NPCs are deleted [6,163]. Specific NTRs preferentially bind specific FG-Nups, hence the presence or absence of certain FG-Nups may affect only specific import routes [6,164,165]. PTM has been reported to change the structure of pores. For example, in yeast, phosphorylation of Nup53 releases its binding partner Nup170, thus exposing binding sites for Kap121 on Nup170, limiting Kap121 import directly [166], a process that may also underlie reduced transport by TRN-1 and Kapβ [127]. Knowing the number and functionality of individual NPCs is a major challenge, and together with the previously mentioned complications of mapping the full complement of NTRS and cognate cargoes in a cell, these aspects provide the largest challenge in interpreting what underlies a change in the localization of a NCT reporter.
To summarize, in order to assess if the transport of proteins is altered in a disease model, well controlled steady state, or dynamic measurements of the location of mobile, non-toxic reporter proteins suffice. Preferably, multiple NLS-or NES-containing reporters representing different transport pathways are used. To understand what drives a possible change in the transport of these reporters, several additional, and rather complex, questions have to be addressed (summarized in Figure 2). In case of the outermost layers, we enter into what is presently still largely uncharted scientific territory. Figure 2. An overview of the questions related to answering whether nucleocytoplasmic transport is altered in a disease model; questions are shown in the top half of the image and methods are shown in the bottom half. The centre circle represents the main question of whether or not NCT is altered; this question can be answered by comparing the localization of transport reporters to either the nuclear or cytosolic compartment in wild type and disease models. The reporters have to be non-toxic, mobile, and preferably multiple NLS-or NES-containing reporters representing different transport pathways are used. To answer how NCT is altered, different additional questions have to be answered represented in layers of increasing complexity. In the case of the outermost layers, we enter into what is presently still largely uncharted scientific territory.
All considerations above apply when comparing data obtained using different model systems. Nucleoporin expression changes between different cell types, tissues, and disease-states [167][168][169][170][171], as well as during development and ageing [172,173]. Moreover, the Figure 2. An overview of the questions related to answering whether nucleocytoplasmic transport is altered in a disease model; questions are shown in the top half of the image and methods are shown in the bottom half. The centre circle represents the main question of whether or not NCT is altered; this question can be answered by comparing the localization of transport reporters to either the nuclear or cytosolic compartment in wild type and disease models. The reporters have to be non-toxic, mobile, and preferably multiple NLS-or NES-containing reporters representing different transport pathways are used. To answer how NCT is altered, different additional questions have to be answered represented in layers of increasing complexity. In the case of the outermost layers, we enter into what is presently still largely uncharted scientific territory.
For the studies related to C9-ALS, a further complication in the comparison of results is related to the fact that the DPRs impact cell physiology variably in the used biological systems as they localize differently and are toxic to different extents. In Table 4, we summarize the localization of different DPRs in different model systems and highlight whether they convey growth defects (indicated in different colours). For example, poly-PR is generally the most toxic DPR and PA is often non-toxic; this is the case in iPSC neurons [194], S. cerevisiae [47], rat neurons [194], mouse neurons, and HEK293 cells [195]. Yet, in zebrafish embryos, PR is less toxic than GR and equally toxic to PA [196]. PR is rarely found in patient material, usually attributed to its high toxicity, but if it is detected, it is found in aggregates in the cytoplasm [197,198]. This localization is not observed in most model systems where PR is nuclear or nucleolar [194,195,[199][200][201][202]. The reports on poly-GA are diverse, reporting non-toxic [46,47,53,[194][195][196]199,200,203,204] as well as toxic [49,200,205,206] effects. Interestingly, it seems that the toxicity of DRPs increases when cells are further differentiated into neurons [207]. Thus, even independent of the discussed cell type specific differences in the nuclear pores and cognate transport factors, the effect of DPRs on transport in the different C9-ALS models may be variable owing to differences in localization and toxicity.

Is Nuclear Transport Altered in C9-ALS?
The seven papers on NCT in C9-ALS [45,50,52,55,[57][58][59] jointly report on 21 experiments assessing the localization of transport reporters in different C9-ALS models (Table 1). Clearly, despite obtaining solid and significant data, it is still difficult to conclude whether the data unambiguously establish that actual effects on NCT kinetics are observed when introducing C9-ALS-related peptides or DNA. How can six papers convincingly show alterations in the localization of transport reporters [45,50,52,55,57,59], whereas the seventh extensively shows no effects can be observed [58]?
Cell type-specific characteristics. When discussing several complications in the interpretation of NCT data, we mentioned cell type-specific transport characteristics, such as distinct NLS-NTR affinities or NTR abundances. This complication is clear when comparing the outcomes of the experiments in B and D (Table 1, for all further references in this section, see Table 1); the same reporter that is excluded from the nucleus in wild type motor neurons localizes to the nucleus in wild type Drosophila salivary glands. The same is observed comparing wild type HeLa Kyoto cells (L) and neuronal cells (N), where the reporter localizes differently in both cell types. These differences depending on cell type are also observed when specific DPRs are introduced. Namely, PR 20 peptide injection reduces importin-α/β import in U2OS cells (F), but not in HeLa Kyoto cells (J). Similarly, poly-GA impacts the transport of an NLS Sv40 -mNeonGreen 2x -NES PKI reporter in neuronal cells (N), but not in HeLa Kyoto cells (L). There may even be subpopulations within a cell type that behave differently. For example, when a subpopulation of cells with stress granules is selected, transport alterations are observed for (L), whereas this was not seen in the whole population [58]. This may be linked to the fact that arginine-rich DPRs can undergo liquid-liquid phase separation, and induce phase separation of a large set of proteins involved in RNA and stress granule metabolism [208]. Jointly, the cell type-specific localization of a reporter in wild type cells illustrates that cell type-specific differences in, among others, NPCs and cognate transport factors impact the transport assays (Table 1, compare L-N, B-D). In addition, the introduction of C9-ALS models adds to the variability between cell types (Table 1, compare F-J, N-L), possibly through the mentioned differences in localization and toxicity (Table 4).
Sorting signals. When discussing the different transport assays available, their possible technical complications were mentioned. A potential issue when using reporters with multiple localization signals relates to the fact that GFP has an intrinsic tendency to accumulate in the nuclear compartment [62,209], irrespective of the presence of an NLS. Nuclear localization of a GFP-based reporter may thus not be driven by import, but rather by influx. For example, the data suggest that the Sv40NLS is not very effective in motor neurons, as it does not promote nuclear accumulation when the NES is removed (E). Without controls, we do not know whether the nuclear accumulation of a reporter is due to import or influx, and the impact of DPRs thus might be on influx rather than active transport. Determining the effect is complicated, as Hayes et al. show that passive diffusion of GFP and small fluorescent dextrans into the nucleus, and thus influx of molecules is increased by PR 10 and GR 10 [50]. Validating the functionality of the sorting signals in reporters with both NLS and NES sequences is thus important to prevent changes in influx being misinterpreted as changes in import.
Transport assays. Changes in transport induced by the introduction of C9-ALS models are quantified in different ways, reporting either the nuclear fluorescence or the cytosolic fluorescence (A-G) or a ratio relative to the total (H-N) or cytosolic (O-P) fluorescence. Measuring the steady state fluorescence in the nucleus relative to the cytosol or total fluorescence is less sensitive to changes in expression level than other readouts such as nuclear (or cytosol) fluorescence alone. This may have impacted the interpretation in this case as poly-PR (and poly-GR) can limit translation [58,204,210]. Hence, it is possible that the expression of the reporter is reduced in the C9-ALS-models (B,C), which caused a lower nuclear fluorescence, rather than an effect on import.
Mobile reporters are the basis of all transport assays, and a quantification of the mobile fraction in FRAP experiments can be used to confirm that they are indeed mobile. However, it is the rate of recovery after bleaching in the nuclear or cytosolic compartment that is a measure for the kinetics of transport. The experiment in (A), for example, measures the change in mobile fraction, rather than actual transport kinetics.
Regarding the choice of transport assays (Table 2) and reporter, we mentioned that it is preferable to assess different transport reporters when studying NCT, as different NTRs each represent unique import pathways with unique parameters-affinities for FG-Nups, expression levels, and competing cargoes-defining their import kinetics. This is illustrated in (H,I) where the localization of a TNPO1 cargo is insensitive to GA 149 , while that of an importin-α/β is sensitive. Moreover, each transport assay has advantages and disadvantages (Table 2), and even though cell permeabilization assays (G) and injections (F,G,J,K) are used frequently in the field, it would be helpful to combine permeabilized studies with live-cell imaging.
Jointly, in the case of these C9-ALS studies, several technical limitations may have impacted the interpretation of the data summarized in Table 1. Hence, at present, it is not firmly established whether the introduction of disease-related biomolecules, G4C2-DNA, RNA, and DPRs, impacts the transport kinetics by NPCs.
Thus, even though convincing data have been obtained confirming a relation to the NCT machinery in C9-ALS in general, it is difficult to conclude from the current transport data if and how C9-ALS affects the actual kinetics of NCT. For future studies, the choice of model systems is critical, both from the perspective of the diverse behaviour of C9-ALS related DPRs (Table 4) and the diversity in the characteristics of NCT in different cells types. Moreover, to facilitate the interpretation of transport assays mechanistically, one would ideally quantify all nucleocytoplasmic transport components (NTR abundance, NPC number and functionality, and the integrity of the Ran gradient), study different NTRs, and combine different transport assays. These in-depth studies are required to answer whether NCT is changed in C9-ALS, and potentially many proteins are mislocalized, leading to cellular alterations causing the disease, or, alternatively, that the NCT machinery is a robust system, and widespread mislocalization of nuclear proteins should not be expected to occur or be causal to the phenotype of C9-ALS. The challenges described are not unique to the case of C9-ALS, and answering the question of how NCT is impacted in neurodegenerative diseases represents a major opportunity for scientists from the nuclear transport and neuroscience communities.  [197,198] (Rare) Cytoplasmic aggregation [198] Cytoplasmic, paranucleolar aggregation [197] Cytoplasmic aggregation [197] Cytoplasmic, (paranuclear) inclusions [205] Paranucleolar aggregation [197] Paranucleolar aggregation [197,205] (Rare) [198] Sparse: Cytoplasmic inclusions, or intra-nuclear inclusions [211] Sparse: Cytoplasmic inclusions, cytoplasmic granular, or intranuclear inclusions [211] Numerous: Cytoplasmic inclusions, cytoplasmic granular, or intranuclear inclusions [211] (Rare) [198] Moderate: Cytoplasmic inclusions or intranuclear inclusions [211] Numerous: Cytoplasmic inclusions, cytoplasmic granular, or intranuclear inclusions [211] Patients spinal chord Nuclear and extra-nuclear inclusions [194] iPSC neurons Nucleolar [194] [ 194] Cytoplasmic diffuse [194,203,212] Perinuclear [212] or cytoplasmic inclusions [194,203] Neuro2a cells Cytoplasmic and nucleolar [213] Cellular diffuse [213] Cellular diffuse [213] Cytoplasmically diffuse [213] Cytosolic and nuclear inclusion bodies [213] [200] [200] [200] [200] [200] Rat neurons Length dependent toxicity [194] [194] [194,214] [194] [194] Nucleolar aggre-gation, cytoplas-mic diffuse [197,214] Cytoplasmic aggregation [206] Mouse neurons Cytoplasmic aggregation [205,213] Cytoplasmic diffuse plus inclusions [195,213] Cellular diffuse [195,213] Cellular diffuse [195,213] Cellular diffuse [195,213] [195]